Creative Group Enterprise Inc

GUDID 00876008005817

Creative Group Enterprise, Inc

Tinted non-prescription spectacles

• Primary Device ID: 00876008005817
• NIH Device Record Key: e1b709da-5e30-45fd-8703-1862fa71c83a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Creative Group Enterprise Inc
• Version Model Number: S Eyewear
• Company DUNS: 117225686
• Company Name: Creative Group Enterprise, Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00876008005817 [Primary]

FDA Product Code

• HQY: Sunglasses (Non-Prescription Including Photosensitive)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-11-24
• Device Publish Date: 2022-11-16

On-Brand Devices [Creative Group Enterprise Inc]

• 00876008005817: S Eyewear
• 00876008005800: R Eyewear